1963
DOI: 10.1093/jaoac/46.2.186
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Rapid Method for Chlorinated Pesticide Residues in Nonfatty Foods

Abstract: Portions of several previously reported methods have been combined, condensed, and modified to provide a rapid, simple procedure for determining chlorinated organic pesticide residues in nonfatty foods. The method is believed to be applicable to 21 pesticides in a variety of foods. Results are reported for 5 pesticides in 11 foods.

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Cited by 58 publications
(49 citation statements)
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“…Improvement of extraction processes, together with the development of analytical methodologies, has lessened the complexity of sample treatment and increased analytical accuracy and precision (Grimalt & Dehouck, 2016). As a fundamental MRM, organochlorine pesticide analysis in foodstuffs (fruits and vegetables) was developed in 1963 using acetonitrile and petroleum ether (Mills, Onley, & Gaither, 1963). To analyse pesticides with greater polarity than the organochlorines, Luke, Froberg, and Masumoto (1975) developed an acetonedependent method followed by the use of dichloromethane and petroleum ether, partitioning and clean-up with florisil.…”
Section: Sample Extractionmentioning
confidence: 99%
“…Improvement of extraction processes, together with the development of analytical methodologies, has lessened the complexity of sample treatment and increased analytical accuracy and precision (Grimalt & Dehouck, 2016). As a fundamental MRM, organochlorine pesticide analysis in foodstuffs (fruits and vegetables) was developed in 1963 using acetonitrile and petroleum ether (Mills, Onley, & Gaither, 1963). To analyse pesticides with greater polarity than the organochlorines, Luke, Froberg, and Masumoto (1975) developed an acetonedependent method followed by the use of dichloromethane and petroleum ether, partitioning and clean-up with florisil.…”
Section: Sample Extractionmentioning
confidence: 99%
“…One-liter water samples, in duplicate, were extracted with hexane. The extract was cleaned on Florisil columns and then combined and concentrated on a Kuderna-Danish sys tem to 1 ml, or sufficiently to achieve a final pesticide concentration of about 2 X 10-7 M. [20][21] Analysis was done on a gas-liquid chromatography unitf equipped with a digital integrator and a strip chart recorder.} Three separate columns were used: (1) 5 per cent QF-1 + 3 per cent DC-200, (2) 1.5 per cent OV-17 + 2 per cent QF-i, and (3) 5 per cent OV-1, all on Chromosorb W 80/100.…”
Section: Experimental Materials and Methodsmentioning
confidence: 99%
“…To obtain different concentrations, 32 different solutions (0, 0.01, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.5, 2, 2.5, 3, 3. 5,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20 times the prescribed dose) were prepared.…”
Section: Strawberry Collection and Pesticide Applicationmentioning
confidence: 99%